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3-oxabicyclo[3.2.1]octan-8-one

Base Information
  • Chemical Name:3-oxabicyclo[3.2.1]octan-8-one
  • CAS No.:625099-16-3
  • Molecular Formula:C7H10O2
  • Molecular Weight:126.155
  • Hs Code.:
3-oxabicyclo[3.2.1]octan-8-one

Synonyms:3-oxabicyclo[3.2.1]octan-8-one

Suppliers and Price of 3-oxabicyclo[3.2.1]octan-8-one
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 3-Oxabicyclo[3.2.1]octan-8-one
  • 25mg
  • $ 2790.00
  • J&W Pharmlab
  • 3-Oxa-bicyclo[3.2.1]octan-8-one 96%
  • 5g
  • $ 9980.00
  • J&W Pharmlab
  • 3-Oxa-bicyclo[3.2.1]octan-8-one 96%
  • 1g
  • $ 2880.00
  • J&W Pharmlab
  • 3-Oxa-bicyclo[3.2.1]octan-8-one 96%
  • 250mg
  • $ 790.00
  • J&W Pharmlab
  • 3-Oxa-bicyclo[3.2.1]octan-8-one 96%
  • 100mg
  • $ 449.00
  • J&W Pharmlab
  • 3-Oxa-bicyclo[3.2.1]octan-8-one 96%
  • 50mg
  • $ 285.00
  • J&W Pharmlab
  • 3-Oxa-bicyclo[3.2.1]octan-8-one 96%
  • 500mg
  • $ 1490.00
  • Crysdot
  • 3-Oxabicyclo[3.2.1]octan-8-one 97%
  • 1g
  • $ 1186.00
Total 5 raw suppliers
Chemical Property of 3-oxabicyclo[3.2.1]octan-8-one
Chemical Property:
  • Boiling Point:214.7±15.0 °C(Predicted) 
  • Density:1.141±0.06 g/cm3(Predicted) 
Purity/Quality:

97% *data from raw suppliers

3-Oxabicyclo[3.2.1]octan-8-one *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 3-Oxabicyclo[3.2.1]octan-8-one is derived from exo-?2,?3-?Epoxynorbornane (E891988), which is a cytotoxic epoxide compound which also may act as a mutagen.
Technology Process of 3-oxabicyclo[3.2.1]octan-8-one

There total 7 articles about 3-oxabicyclo[3.2.1]octan-8-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrogenchloride; water; at 20 ℃;
Guidance literature:
Multi-step reaction with 3 steps
1: silver(l) oxide / potassium iodide / dichloromethane / 72 h / 20 °C
2: potassium carbonate / methanol / 20 °C
3: hydrogenchloride; water / 20 °C
With hydrogenchloride; water; potassium carbonate; silver(l) oxide; potassium iodide; In methanol; dichloromethane;
Guidance literature:
Multi-step reaction with 6 steps
1.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 °C
1.2: 0.5 h / -78 - 20 °C
2.1: toluene-4-sulfonic acid / benzene / 4 h / Reflux
3.1: ozone / dichloromethane; methanol / -78 °C
3.2: -78 - 0 °C
4.1: silver(l) oxide / potassium iodide / dichloromethane / 72 h / 20 °C
5.1: potassium carbonate / methanol / 20 °C
6.1: hydrogenchloride; water / 20 °C
With hydrogenchloride; oxalyl dichloride; water; potassium carbonate; toluene-4-sulfonic acid; ozone; dimethyl sulfoxide; silver(l) oxide; potassium iodide; In methanol; dichloromethane; benzene;
upstream raw materials:

C9H16O4

C16H22O6S

anti-bicyclo<2.2.1>hept-2-en-7-ol

7-norbornenone

Downstream raw materials:

C18H21NO5

C18H23NO5

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